Descrizione dell'offerta
Location
Rozzano
Company Randstad Italia, specialty Pharma, search for an important pharmaceutical company producing finished products, a Laboratory Analyst R&D.
Position Laboratory Analyst R&D
Contract & Benefits Initial contract in manufacturing with possibility of progression and personnel growth, CCNL Chimico aziende industriali livello D, 13 mensilità, ticket restaurant.
Working Hours Full time 37h45min, Monday to Friday (daily schedule).
Salary Annual: 22,000€ - 28,000€
Experience 1 year
Responsibilities
Follow complex analytical activities on finished products APIs (Active Principles) following priority defined by the Laboratory Manager.
Draft the report protocol of validation and analytical transfer (method of the laboratory intern QA).
Responsible for the control of the devices and analysis schedule, ensuring maximum document accuracy.
Collaborate on the SOP management of laboratory unit and on the handling of analytical equipment (calibration and periodic control).
Qualifications
Degree in Chemistry, Pharmacy or Biotechnology.
At least 1 year of experience as an analyst in the chemical–physical (QCoR&D) field.
Proficiency in HPLC, GC, Solubility Systems and UV Spectrophotometry.
Orientation to data, precision and ability to operate according to rigid quality standards.
Educational Level University degree (3 years) or equivalent.
La ricerca è rivolta ai candidati ambosessi (L.903/77).
#J-18808-Ljbffr
Company Randstad Italia, specialty Pharma, search for an important pharmaceutical company producing finished products, a Laboratory Analyst R&D.
Position Laboratory Analyst R&D
Contract & Benefits Initial contract in manufacturing with possibility of progression and personnel growth, CCNL Chimico aziende industriali livello D, 13 mensilità, ticket restaurant.
Working Hours Full time 37h45min, Monday to Friday (daily schedule).
Salary Annual: 22,000€ - 28,000€
Experience 1 year
Responsibilities
Follow complex analytical activities on finished products APIs (Active Principles) following priority defined by the Laboratory Manager.
Draft the report protocol of validation and analytical transfer (method of the laboratory intern QA).
Responsible for the control of the devices and analysis schedule, ensuring maximum document accuracy.
Collaborate on the SOP management of laboratory unit and on the handling of analytical equipment (calibration and periodic control).
Qualifications
Degree in Chemistry, Pharmacy or Biotechnology.
At least 1 year of experience as an analyst in the chemical–physical (QCoR&D) field.
Proficiency in HPLC, GC, Solubility Systems and UV Spectrophotometry.
Orientation to data, precision and ability to operate according to rigid quality standards.
Educational Level University degree (3 years) or equivalent.
La ricerca è rivolta ai candidati ambosessi (L.903/77).
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
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